Partner
BioEgypt
PTS Diagnostics lists BioEgypt in its distributor directory for Egypt.
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Partner
PTS Diagnostics lists BioEgypt in its distributor directory for Egypt.
Partner
PTS Diagnostics lists BioLab Internacional, S.A. in its distributor directory for Panama.
Partner
PTS Diagnostics lists Biosite Medical Instruments, Inc. – Manila Office in its distributor directory for Philippines.
Partner
PTS Diagnostics lists Biosynex Ibérica in its distributor directory for Spain, Portugal.
Article
Research record from ACS Sens, 2026-07-01. PMID 42405683.
Partner
GeneProof lists BS Diagnostics in its distributor directory for Tunisia.
Indicators
An antigen expressed by tissues derived from mullerian epithelium (tubal, endometrial and endocervical) or celomic epithelium (mesothelial cells of the pleura, pericardium and peritoneum). Although its biochemical nature has not been clearly defined, CA125 has been described as a glycosylated, high-molecular-weight protein that may be released from damaged cells. Measurable in plasma, CA125 is a sensitive, nonspecific tumor marker for ovarian cancer; as such it is much more useful for monitoring clinical responses to the treatment of ovarian cancer than for the diagnosis of ovarian cancer. Elevated plasma CA125 may occur in association with other malignancies and non-malignant gynecologic disorders. (NCI04)
Article
Research record from Diagnostics (Basel), 2026-03-27. PMID 41975718.
Article
Research record from Front Oncol, 2026-03-04. PMID 41858343.
Article
A composite case study on MRSA screening: how late reporting happens, the diagnostic decisions that close the gap, and how to verify the fix with measurable targets.
Tests
This test looks for CCP (cyclic citrullinated peptide) antibodies in your blood. CCP antibodies, also called anti-CCP antibodies, are a type of antibody called autoantibodies. Antibodies and autoantibodies are proteins made by the immune system :
Glossary Term
A manufacturer declaration that an in vitro diagnostic complies with applicable EU legislation (the IVDR since May 2022). CE-IVD indicates regulatory conformance, not a statement of clinical superiority; buyers still review performance claims and intended use.